chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141125716411257165AG20GENIChomozygous113340326
141125736611257367AT28GENIChomozygous113340328
141125894711258948TG29GENIChomozygous113340330
141125928511259286GA39GENIChomozygous113340332
141125980911259810AG33GENIChomozygous113340334
141126002511260026AG19GENIChomozygous113340336
141126002811260029CT20GENIChomozygous113340338
141126038511260386TA29GENIChomozygous113340340
141126069711260698CT35GENIChomozygous113340342
141126148911261490CT25GENIChomozygous113340344
141126237211262373TC32GENIChomozygous113340348
141126243311262434CT25GENIChomozygous113340350
141126364911263650CT13GENIChomozygous113340352
141126456711264568TC37GENIChomozygous113340356
141126458311264584TG33GENIChomozygous113340358
141126462111264622GA27GENIChomozygous113340362
141126514111265142CG35GENIChomozygous113340364
141126524911265250CG35GENIChomozygous113340366
141126540111265402GA26GENIChomozygous113340368
141126679111266792TC29GENIChomozygous113340372
141126754611267547AT28GENIChomozygous113340374
141126771911267720CA8GENIChomozygous113574630
141126783711267838AG33GENIChomozygous113340377
141126897811268979AG16GENIChomozygous113340379
141126911511269116CT28GENIChomozygous113340381
141126937911269380CT33GENIChomozygous113340383
141126939511269396GA32GENIChomozygous113340385
141126998411269985TC43GENIChomozygous113340387
141127080111270802AG34GENIChomozygous113340389
141127081211270813GA36GENIChomozygous113340391
141127133911271340TC25GENIChomozygous113340393
141127243511272436CT26GENIChomozygous113340395
141127264411272645CT22GENIChomozygous113574633
141127272511272726CT31GENIChomozygous113340397
141127290811272909AG26GENIChomozygous113340399
141127467411274675GA23GENIChomozygous113340401